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1.
Lung Cancer ; 107: 100-107, 2017 05.
Article in English | MEDLINE | ID: mdl-27180141

ABSTRACT

Lung cancer is the predominant cause of cancer-related mortality in the world. The majority of patients present with locally advanced or metastatic non-small-cell lung cancer (NSCLC). Treatment for NSCLC is evolving from the use of cytotoxic chemotherapy to personalized treatment based on molecular alterations. Unfortunately, the quality of the available tumor biopsy and/or cytology material is not always adequate to perform the necessary molecular testing, which has prompted the search for alternatives. This review examines the use of circulating cell-free nucleic acids (cfNA), consisting of both circulating cell-free (tumoral) DNA (cfDNA-ctDNA) and RNA (cfRNA), as a liquid biopsy in lung cancer. The development of sensitive and accurate techniques such as Next-Generation Sequencing (NGS); Beads, Emulsion, Amplification, and Magnetics (BEAMing); and Digital PCR (dPCR), have made it possible to detect the specific genetic alterations (e.g. EGFR mutations, MET amplifications, and ALK and ROS1 translocations) for which targeted therapies are already available. Moreover, the ability to detect and quantify these tumor mutations has enabled the follow-up of tumor dynamics in real time. Liquid biopsy offers opportunities to detect resistance mechanisms, such as the EGFR T790M mutation in the case of EGFR TKI use, at an early stage. Several studies have already established the predictive and prognostic value of measuring ctNA concentration in the blood. To conclude, using ctNA analysis as a liquid biopsy has many advantages and allows for a variety of clinical and investigational applications.


Subject(s)
Biomarkers, Tumor/blood , Carcinoma, Non-Small-Cell Lung/pathology , Cell-Free Nucleic Acids/blood , Liquid Biopsy/methods , Lung Neoplasms/pathology , Precision Medicine/methods , Biomarkers, Tumor/genetics , Blood Platelets/pathology , Carcinoma, Non-Small-Cell Lung/blood , Carcinoma, Non-Small-Cell Lung/genetics , Carcinoma, Non-Small-Cell Lung/therapy , Cell-Free Nucleic Acids/genetics , DNA, Neoplasm/blood , Drug Resistance, Neoplasm , ErbB Receptors/genetics , Genomics , High-Throughput Nucleotide Sequencing , Humans , Lung Neoplasms/blood , Lung Neoplasms/genetics , Lung Neoplasms/therapy , Mutation , Neoplasm Staging , Prognosis , Protein Kinase Inhibitors/therapeutic use
2.
Pharmacol Ther ; 155: 1-10, 2015 Nov.
Article in English | MEDLINE | ID: mdl-26213107

ABSTRACT

Over the last decades, advances in the knowledge of immunology have led to the identification of immune checkpoints, reinvigorating cancer immunotherapy. Although normally restricted to activated T and B cells, constitutive expression of CD70 in tumor cells has been described. Moreover, CD70 is implicated in tumor cell and regulatory T cell survival through interaction with its ligand, CD27. In this review, we summarize the targetable expression patterns of CD70 in a wide range of malignancies and the promising mechanism of anti-CD70 therapy in stimulating the anti-tumor immune response. In addition, we will discuss clinical data and future combination strategies.


Subject(s)
CD27 Ligand/immunology , Immunotherapy , Neoplasms/therapy , Animals , Humans , Neoplasms/immunology
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